Parexel - IT - Administration

Parexel seeks a US/Canadian Board-certified Ophthalmologist to join as a Medical Director. Provide expert medical monitoring, client consultation, and leadership in global ophthalmic drug development. Enjoy a flexible, remote role with a focus on professional growth and a client-focused approach.

Join Parexel in Germany as a Study Physician for key Oncology trials. Provide medical oversight from protocol design to final report, ensuring high-quality data. Requires an MD with 4+ years of clinical practice and ideally industry/CRO experience. This core role offers a chance to shape clinical...

Lead a clinical operations team in Bengaluru, ensuring high-quality, on-time project delivery. Utilize your substantial clinical research experience to manage, resource, and develop professionals. Drive project success through oversight, consultation, and client liaison in a dynamic CRO environment.

Join Parexel as a Document Specialist, supporting critical clinical research from a remote Canada position. Utilize your expertise in clinical document formatting and publishing software to ensure submission-ready deliverables. This role offers continuous learning, career growth, and a patient-fo...

Lead centralized monitoring for global clinical trials as a Manager, Data Analysis. Configure and maintain RBQM systems, utilizing programming expertise in R, SQL, or SAS for advanced data analysis and KRI/KPI reporting. This US-based role requires 4+ years of pharma experience and direct RBQM sy...

Lead cross-functional clinical trial teams as a Project Specialist at Parexel in Colombia. Utilize your strong project management, Excel, and English skills to drive study delivery and financial metrics. Enjoy a flexible, supportive environment with professional growth opportunities while helping...

Lead global clinical trial site activation for a pharmaceutical sponsor. Utilize your 4-6 years of regulatory submission and project management experience in Pharma/CRO. Based in Serbia, you will develop strategies, oversee CRO performance, and ensure efficient, compliant study start-up.

Join Parexel FSP as a Junior Clinical Trial Manager in a home-based role in Spain. You will manage clinical trials, oversee vendors, and ensure GCP compliance. This role offers exceptional financial rewards and development while dedicated to a single sponsor. Utilize your CRA experience in a posi...

Join Parexel as a Regulatory CMC Project Manager. Utilize your 3+ years of CMC regulatory experience to manage complex submissions and strategic plans for biopharma clients. Enjoy a fully remote role with East Coast hours, career growth, and expert mentorship. Be part of a supportive team shaping...

Join Parexel as a Veeva Clinical Digital Systems Analyst in Poland. You will optimize clinical trial processes by managing digital systems, bridging technology and operations. This role requires 5+ years in clinical technology and offers a performance bonus, career development, and a friendly wor...

Lead IT Operations and Service Desk teams in Hyderabad. Utilize your 6-8 years of IT infrastructure experience and 4-6 years in people management to ensure network uptime and swift issue resolution. Drive continuous improvement, manage escalations, and develop a team of 15 direct reports in this ...

Join Parexel as a Data Surveillance Analyst. Utilize your clinical data experience and SAS/SQL skills to analyze trends and manage risks in a fully flexible, home-based role. You will develop Data Surveillance Plans and present key findings, ensuring study quality and patient welfare. We offer co...